166375
Formic hydrazide
Synonym(s):
Formic acid hydrazide, Formylhydrazine
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About This Item
Linear Formula:
HCONHNH2
CAS Number:
Molecular Weight:
60.06
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-867-9
Beilstein/REAXYS Number:
635759
MDL number:
InChI key
XZBIXDPGRMLSTC-UHFFFAOYSA-N
InChI
1S/CH4N2O/c2-3-1-4/h1H,2H2,(H,3,4)
SMILES string
[H]C(=O)NN
mp
52-57 °C (lit.)
solubility
water: soluble 2.5%, clear, colorless
functional group
amine
hydrazine
Quality Level
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Application
Formic hydrazide was used in the synthesis of 1,2,4-triazole derivatives. It was also used in the synthesis of new anticancer agent, 6-N-formylamino-12,13-dihydro-1,11-dihydroxy-13-(β-D-glucopyranosyl)-5H-indolo[2,3-a]-pyrrolo[3,4-c]carbazole-5,7(6H)-dione.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
233.6 °F - closed cup
flash_point_c
112 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Synthesis of NB-506, a new anticancer agent.
Ohkubo M, et al.
Tetrahedron, 53(2), 585-592 (1997)
B Toth et al.
Carcinogenesis, 1(1), 61-65 (1980-01-01)
N-ethyl-N-formylhydrazine (EFH) was administered as a 0.02% solution in drinking water continuously for life to randomly bred Swiss mice, from 6 weeks of age. The treatment induced tumors of the lungs, blood vessels, liver, gall bladder and preputial glands. The
Traceless liquid-phase synthesis of 3-alkylamino-4, 5-disubstituted-1, 2, 4-triazoles on polyethylene glycol (PEG).
Zong Y-X, et al.
Tetrahedron Letters, 46(31), 5139-5141 (2005)
Coro Echeverría et al.
Polymers, 11(6) (2019-06-05)
Nano-sized one-dimensional metallo-organic polymers, characterized by the phenomenon of spin transition, are excellent candidates for advanced technological applications such as optical sensors, storage, and information processing devices. However, the main drawback of this type of polymers is their fragile mechanical
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